홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

O-Xylene → Acetic acid 2-(aminothioxomethyl)-1-(4-methoxyphenyl)hydrazide

HRID 904001
노트
인쇄 미리보기

반응식

HRID 904001 반응식
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([NH:9][NH:10][C:11](=[S:13])[NH2:12])=[CH:5][CH:4]=1.[C:14](OC(=O)C)(=[O:16])[CH3:15].CC1C=CC=CC=1C.O(C(C)C)C(C)C>O>[NH2:12][C:11](=[S:13])[NH:10][N:9]([C:6]1[CH:5]=[CH:4][C:3]([O:2][CH3:1])=[CH:8][CH:7]=1)[C:14](=[O:16])[CH3:15]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 7237O-XyleneHCID 7914Diisopropyl EtherHCID 7918Acetic AnhydrideHCID 28261724-Methoxyphenylthiosemicarbazide

생성물 1

HCID 54330889Acetic acid 2-(aminothioxomethyl)-1-(4-methoxyphenyl)hydrazide수율 89%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

A mixture of 17.5 parts of 2-(4-methoxyphenyl)hydrazinecarbothioamide, 10 parts of acetic acid anhydride and 90 parts of dimethylbenzene is stirred and refluxed for one hour. The reaction mixture is allowed to cool to room temperature and 2,2'-oxybispropane and water are added. The precipitated product is filtered off and dried, yielding 14.5 parts (89%) of acetic acid 2-(aminothioxomethyl)-1-(4-methoxyphenyl)hydrazide.

후처리

  1. temperaturerefluxed for one hour
  2. filtrationThe precipitated product is filtered off
  3. customdried

출처 및 근거

ORD 기록
ord-9cb19ca09af34633b85ee82e1a61d51c
출처 데이터셋
uspto-grants-1980_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04229581

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트